Canonical Allele Identifier: CA412568100
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047196G>T , CM000685.2:g.22047196G>T GRCh38
NC_000023.10:g.22065314G>T , CM000685.1:g.22065314G>T GRCh37
NC_000023.9:g.21975235G>T NCBI36
NG_007563.2:g.19394G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.760G>T
ENST00000683214.1:n.544+14073G>T
ENST00000684143.1:c.334G>T ENSP00000508264.1:p.Asp112Tyr
ENST00000379374.5:c.334G>T MANE Select ENSP00000368682.4:p.Asp112Tyr
ENST00000379374.4:c.334G>T ENSP00000368682.4:p.Asp112Tyr
NM_000444.5:c.334G>T NP_000435.3:p.Asp112Tyr
NM_001282754.1:c.334G>T NP_001269683.1:p.Asp112Tyr
XM_011545535.1:c.334G>T XP_011543837.1:p.Asp112Tyr
XM_017029579.1:c.-109G>T XP_016885068.1:n.-109G>T
XM_024452390.1:c.43G>T XP_024308158.1:p.Asp15Tyr
XR_001755695.1:n.1013G>T
NM_000444.6:c.334G>T MANE Select NP_000435.3:p.Asp112Tyr
NM_001282754.2:c.334G>T NP_001269683.1:p.Asp112Tyr